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Urgent Referral

Fetal Conditions

Spina Bifida & Neural Tube Defects

Reviewed by: Dr. Ali Al-Ibrahim
13 min read
Last reviewed: 2026-08-26
Selected CasesPrenatal Repair
Lemon/Banana SignBrain Signs
Alpha-FetoproteinKey Marker
Fetoscopic/OpenFetal Surgery

In brief — the direct answer

Spina bifida is a neural-tube defect in which the spine and spinal cord do not form normally early in pregnancy. It can affect mobility, bladder and bowel function, and brain development. Care begins with accurate diagnosis and multidisciplinary counselling. Postnatal repair remains an established pathway; prenatal repair may be considered only for carefully selected cases at an appropriately governed specialist centre.

What is Spina Bifida & Neural Tube Defects?

The most common form is Myelomeningocele, where a sac of fluid containing spinal nerves protrudes through an opening in the back. Because the nerves are exposed to the amniotic fluid, they become damaged over time.

Spina Bifida also affects the brain through a mechanism called the Chiari II Malformation. Because of the opening in the spine, the fluid around the brain 'leaks' down, causing the base of the brain (the cerebellum) to be pulled downwards. This creates the classic 'Banana Sign' and 'Lemon Sign' (the shape of the baby's head) that we see on ultrasound.

Who is at risk?

The primary risk factor for NTDs is a deficiency in Folic Acid (Vitamin B9) during the very first weeks of pregnancy, often before a woman knows she is pregnant.

  • Other risks include certain maternal medications (like anti-seizure drugs) or pre-existing maternal diabetes.
  • If you have had one pregnancy affected by Spina Bifida, your risk for future pregnancies increases, and we recommend a much higher dose of Folic Acid (5mg) starting 3 months before conception.

How we diagnose it

Most cases are diagnosed during the 20-week anomaly scan, though subtle brain signs can often be seen as early as 12-13 weeks.

  1. Brain Markers: The 'Lemon Sign' (flattening of the forehead) and the 'Banana Sign' (curved cerebellum) are highly accurate screening markers.
  2. Spinal Level: We meticulously scan every vertebra to determine the 'level' of the defect (e.g., L3 or S1). The lower the defect is on the spine, the better the prognosis for walking.
  3. Limb Movement: We observe the baby's leg and foot movements (checking for 'clubfoot' or reduced motion).

What does management involve?

After diagnosis, the team maps the lesion, assesses the brain and other anatomy, offers genetic evaluation where appropriate, and discusses likely mobility, bladder and bowel function, hydrocephalus, delivery, and neonatal care. Options may include postnatal repair or referral to a specialist fetal-surgery centre for prenatal-repair assessment. Any prenatal intervention requires strict multidisciplinary selection, institutional approval, detailed consent, appropriate research or innovation governance, prospective registration, and outcome audit.

What are the outcomes?

Children with Spina Bifida can lead long, fulfilling lives.

  • Mobility: Many children learn to walk, though some may require braces or a wheelchair if the defect is high on the spine.
  • Brain Health: Prenatal surgery significantly reduces the risk of needing a 'shunt' for hydrocephalus.
  • Cognition: Most children with Spina Bifida have normal intelligence, though they may face specific learning challenges related to spatial reasoning.
  • Multidisciplinary Care: These children require a life-long team including urologists, orthopedists, and neurosurgeons.

When to see a subspecialist

Suspected spina bifida should be referred promptly to Maternal-Fetal Medicine for confirmation, full anatomical assessment, genetic counselling, and multidisciplinary planning. Where prenatal repair might be relevant, we coordinate assessment with an appropriately governed specialist programme; Fetus.ae does not present prenatal repair as a routine service of our unit.

Questions to ask your doctor

This depends on the level of the defect and whether fetal surgery is performed. Babies with defects lower in the spine (sacral) have a much higher chance of walking independently than those with higher (thoracic) defects.
The landmark MOMS trial showed that babies who had surgery in the womb were twice as likely to walk independently and were significantly less likely to need a brain shunt after birth.
Occulta is usually a very mild form that is covered by skin. It often has no brain signs and a very good prognosis, sometimes not being discovered until adulthood.
It reduces the risk by over 70%, but it does not eliminate it entirely, as some cases are caused by other genetic or environmental factors.
Dr. Ali Al-Ibrahim
Content Reviewer

Dr. Ali Al-Ibrahim

Head of Unit, Consultant Maternal Fetal Medicine

Consultant in Maternal-Fetal Medicine in Al Ain and Abu Dhabi with more than 25 years of experience, University of Toronto fellowship training, and Arab and Saudi Board certification in OBGYN.

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References & Clinical Guidelines

  1. ISUOG Practice Guidelines: sonographic examination of the fetal central nervous system — ISUOG (2020)
  2. Neural Tube Defects (Practice Bulletin 187) — ACOG (2017)
  3. A Randomized Trial of Prenatal versus Postnatal Repair of Myelomeningocele (MOMS trial) — Adzick et al. NEJM (2011)
  4. Maternal-Fetal Surgery for Myelomeningocele (Committee Opinion 720) — ACOG / SMFM (2017)
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